Insights into the Role of Nanorod-Shaped MnO₂ and CeO₂ in a Plasma Catalysis System for Methanol Oxidation

Abstract

Published papers highlight the roles of the catalysts in plasma catalysis systems, and it is essential to provide deep insight into the mechanism of the reaction. In this work, a coaxial dielectric barrier discharge (DBD) reactor packed with γ-MnO2 and CeO2 with similar nanorod morphologies and particle sizes was used for methanol oxidation at atmospheric pressure and room temperature. The experimental results showed that both γ-MnO2 and CeO2 exhibited good performance in methanol conversion (up to 100%), but the CO2 selectivity of CeO2 (up to 59.3%) was much higher than that of γ-MnO2 (up to 28.6%). Catalyst characterization results indicated that CeO2 contained more surface-active oxygen species, adsorbed more methanol and utilized more plasma-induced active species than γ-MnO2. In addition, in situ Raman spectroscopy and Fourier transform infrared spectroscopy (FT-IR) were applied with a novel in situ cell to reveal the major factors affecting the catalytic performance in methanol oxidation. More reactive oxygen species (O22−, O2−) from ozone decomposition were produced on CeO2 compared with γ-MnO2, and less of the intermediate product formate accumulated on the CeO2. The combined results showed that CeO2 was a more effective catalyst than γ-MnO2 for methanol oxidation in the plasma catalysis system.

Keywords

• methanol oxidation
• plasma catalysis
• CeO₂
• MnO₂
• in situ ft-IR